Result

Search results for the GEO ID: GSE35825

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GSM ID

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Title

Source name

Description

Characteristics

GSM875786

GPL1261

Media rep1

Bone marrow macrophages, untreated (media only)

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: none

Sample_geo_accession	GSM875786
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875786/suppl/GSM875786.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875786/suppl/GSM875786.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875787

GPL1261

Media rep2

Bone marrow macrophages, untreated (media only)

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: none

Sample_geo_accession	GSM875787
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875787/suppl/GSM875787.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875787/suppl/GSM875787.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875788

GPL1261

Media rep3

Bone marrow macrophages, untreated (media only)

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: none

Sample_geo_accession	GSM875788
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875788/suppl/GSM875788.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875788/suppl/GSM875788.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875789

GPL1261

IFNa rep1

Bone marrow macrophages treated with IFNa (62U/mL) for 2.5hrs

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: interferon-alpha

Sample_geo_accession	GSM875789
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875789/suppl/GSM875789.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875789/suppl/GSM875789.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875790

GPL1261

IFNa rep2

Bone marrow macrophages treated with IFNa (62U/mL) for 2.5hrs

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: interferon-alpha

Sample_geo_accession	GSM875790
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875790/suppl/GSM875790.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875790/suppl/GSM875790.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875791

GPL1261

IFNa rep3

Bone marrow macrophages treated with IFNa (62U/mL) for 2.5hrs

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: interferon-alpha

Sample_geo_accession	GSM875791
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875791/suppl/GSM875791.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875791/suppl/GSM875791.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875792

GPL1261

IFNg rep1

Bone marrow macrophages treated with IFNg (1U/mL) for 2.5hrs

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: interferon-gamma

Sample_geo_accession	GSM875792
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875792/suppl/GSM875792.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875792/suppl/GSM875792.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875793

GPL1261

IFNg rep2

Bone marrow macrophages treated with IFNg (1U/mL) for 2.5hrs

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: interferon-gamma

Sample_geo_accession	GSM875793
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875793/suppl/GSM875793.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875793/suppl/GSM875793.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

GSM875794

GPL1261

IFNg rep3

Bone marrow macrophages treated with IFNg (1U/mL) for 2.5hrs

strain: C57BL/6J Sex: female age: 6 weeks tissue: bone marrow-derived macrophages treatment: interferon-gamma

Sample_geo_accession	GSM875794
Sample_status	Public on Feb 15 2012
Sample_submission_date	Feb 14 2012
Sample_last_update_date	Feb 15 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	IFNa and IFNg was resuspended in DMEM and added to day 7 BMM in growth media to a final concentration 62U/mL and 1U/mL, respectively. After 2.5 hours, the media was removed and the cells were collected in 1mL of TRIzol (Invitrogen) and further processed for RNA purification.
Sample_growth_protocol_ch1	Bone marrow was harvested from the femur of mice and plated in 10cm dishes in Dulbecco's MEM (Gibco), 10%FBS, 1% Penicillin/Streptomycin and ~10ng/mL of M-CSF for 7 days. The media was refreshed on day 4.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	Cy3
Sample_label_protocol_ch1	Cy3 cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization was performed according to the manufacturer's instructions.
Sample_scan_protocol	GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Sample_data_processing	The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
Sample_platform_id	GPL1261
Sample_contact_name	Su-Yang,,Liu
Sample_contact_laboratory	Genhong Cheng
Sample_contact_department	Microbiology, Immunology, and Molecular Genetics
Sample_contact_institute	University of California, Los Angeles
Sample_contact_address	615 Charles E. Young Dr. South Rm 246
Sample_contact_city	Los Angeles
Sample_contact_state	CA
Sample_contact_zip/postal_code	90095
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875794/suppl/GSM875794.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM875nnn/GSM875794/suppl/GSM875794.CHP.gz
Sample_series_id	GSE35825
Sample_data_row_count	45101

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